A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520391



Internal ID15447684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36473993..36527313hg38UCSC Ensembl
Innerchr8:36331511..36384831hg19UCSC Ensembl
Innerchr8:36450669..36503989hg18UCSC Ensembl
Innerchr8:36450669..36503989hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3853321
hg1953321
hg1853321
hg1753321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697387
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520391
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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